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[小儿患者甲氨蝶呤所致神经毒性。临床症状及神经影像学表现描述]

[Neurotoxicity due to methotrexate in paediatric patients. Description of the clinical symptoms and neuroimaging findings].

作者信息

Garcia-Puig Montserrat, Fons-Estupina M Carmen, Rives-Sola Susana, Berrueco-Moreno Rubén, Cruz-Martinez Ofelia, Campistol Jaume

机构信息

Servicio de Neurología, Hospital Sant Joan de Deu, Esplugues de Llobregat, Spain.

出版信息

Rev Neurol. 2012 Jun 16;54(12):712-8.

Abstract

INTRODUCTION. High-dose methotrexate (MTX) has showed to increase the surveillance in children with acute lymphoblastic leukemia and other neoplasms. However, MTX may induce significant neurotoxicity. AIM. To evaluate, in our population of patients who have been treated with MTX, the incidence of neurotoxicity and to describe its main clinical and radiological characteristics. PATIENTS AND METHODS. We retrospectively review the patients who received treatment with systemic high-dose MTX and/or intrathecal MTX between 1994 and 2010. The children who presented clinical o radiological signs of neurotoxicity were reviewed. RESULTS. We identified 284 patients who received high-dose intravenous and/or intrathecal MTX. 9 patients presented neurotoxicity. The median age at diagnosis was 6 years; 6 patients were male. The diagnosis included: 6 acute lymphoblastic leukemia, 2 medulloblastoma and 1 lymphoma. 66% patients presented focal neurological dysfunction, 3 had non-specific symptoms. In 5 patients the symptomatology started the first 14 days after the MTX administration. 8 patients had complete clinical resolution, but only one presented neurological long term effects. All the patients except one showed signs of acute leukoencephalopathy in the brain MR study. These alterations resolved one year later in 3 patients; in the other patients the MR alterations persisted. The neurotoxicity management was corticosteroid, folinic acid, aminophylline and dextromethorphan. CONCLUSION. The MTX neurotoxicity it can present as acute or chronic. It has a wide clinical spectrum, ranging from sub-clinical manifestations with complete recovery to a chronic and progressive encephalopathy.

摘要

引言。大剂量甲氨蝶呤(MTX)已被证明可加强对急性淋巴细胞白血病及其他肿瘤患儿的监测。然而,MTX可能会诱发显著的神经毒性。目的。评估在我们接受MTX治疗的患者群体中神经毒性的发生率,并描述其主要的临床和放射学特征。患者与方法。我们回顾性分析了1994年至2010年间接受全身大剂量MTX和/或鞘内注射MTX治疗的患者。对出现神经毒性临床或放射学征象的患儿进行了复查。结果。我们确定了284例接受大剂量静脉和/或鞘内注射MTX的患者。9例出现神经毒性。诊断时的中位年龄为6岁;6例为男性。诊断包括:6例急性淋巴细胞白血病、2例髓母细胞瘤和1例淋巴瘤。66%的患者出现局灶性神经功能障碍,3例有非特异性症状。5例患者的症状在MTX给药后的前14天开始出现。8例患者临床症状完全缓解,但只有1例有长期神经影响。除1例患者外,所有患者在脑部磁共振成像研究中均显示急性白质脑病征象。3例患者的这些改变在1年后消失;其他患者的磁共振成像改变持续存在。神经毒性的治疗方法为使用皮质类固醇、亚叶酸、氨茶碱和右美沙芬。结论。MTX神经毒性可表现为急性或慢性。其临床谱广泛,从完全恢复的亚临床表达到慢性进行性脑病不等。

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